Z-1917-2024 Class II Ongoing
FDA device recall Z-1917-2024 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Mar 1, 2024 and is designated Class II. Reason for recall: Trumpet Needle Guide ring can detach when excessive pressure is applied. The recall status is ongoing. Affected quantity: 30 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 5, 2024
- Initiation Date
- Mar 1, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 30 units
Product Description
Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray
Reason for Recall
Trumpet Needle Guide ring can detach when excessive pressure is applied.
Distribution Pattern
US Nationwide distribution.
Code Information
UDI/DI 40653160122945 (case), 10653160122944 (unit), Lot Numbers: 23JBX257, 23KMG455
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1917-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026